Subject(s)
Delayed Diagnosis , HIV Infections/diagnosis , HIV , Tuberculosis, Pulmonary/therapy , Adult , Aged, 80 and over , Delayed Diagnosis/prevention & control , HIV/isolation & purification , HIV Infections/complications , Humans , Male , Risk Factors , Treatment Outcome , Tuberculosis, Pulmonary/diagnosis , Tuberculosis, Pulmonary/etiologyABSTRACT
We have previously reported that lymphoid cells from systemic lupus erythematosus (SLE) mice with established disease migrate aberrantly. This study evaluates the abnormal lymphocyte migration patterns found in MRL-lpr/lpr (MRL/l) mice in relation to age, disease manifestations and the expression of lymphocyte homing receptors. 51chromium-labelled lymph node cells from MRL/l and from normal histocompatible CBA mice of different ages were injected i.v. into age and sex-matched CBA recipients. Diminished lymph node and increased hepatic uptake of MRL/l compared to CBA cells was evident as early as 6 weeks of age. Abnormalities in lymphocyte migration antedated the appearance of elevated antihistone antibody (AHA) levels but not the development of lymphadenopathy. Using the monoclonal antibody MEL-14, no differences in the expression of lymphocyte homing receptors between MRL/l and CBA lymph node cells were found at any age. Thus abnormalities in lymphocyte migration in MRL/l mice appear as early as six weeks and are not related to changes in homing receptor expression.
Subject(s)
Autoimmune Diseases/immunology , Lymphocytes/immunology , Receptors, Lymphocyte Homing/metabolism , Age Factors , Animals , Autoantibodies/blood , Autoimmune Diseases/pathology , Cell Movement/immunology , Histones/immunology , Lupus Erythematosus, Systemic/immunology , Lupus Erythematosus, Systemic/pathology , Lymph Nodes/immunology , Lymph Nodes/pathology , Lymphocytes/pathology , Lymphocytes/physiology , Mice , Mice, Mutant StrainsABSTRACT
The patterns of migration of lymphoid cells from autoimmune-prone MRL-lpr/lpr, C57BL/6-lpr/lpr, MRL-+/+, and NZB mice were compared to those from sex and age-matched, normal CBA, C57BL/6, and BALB/C mice. Chromium-51-labelled spleen and lymph node cells from all autoimmune mice tested homed preferentially to the spleen relative to lymph node of the recipient strain. The data indicate that defects in lymphocyte trafficking are widespread in murine lupus and suggest a role for abnormal lymphocyte migration in the pathogenesis of this disease.
